Canonical Allele Identifier: CA2261365494

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374952_44374971delinsTCCCCGCCCAGAAGGCCCGG , CM000679.2:g.44374952_44374971delinsTCCCCGCCCAGAAGGCCCGG	GRCh38
NC_000017.10:g.42452320_42452339delinsTCCCCGCCCAGAAGGCCCGG , CM000679.1:g.42452320_42452339delinsTCCCCGCCCAGAAGGCCCGG	GRCh37
NC_000017.9:g.39807846_39807865delinsTCCCCGCCCAGAAGGCCCGG	NCBI36
NG_008331.1:g.19535_19554delinsCCGGGCCTTCTGGGCGGGGA , LRG_479:g.19535_19554delinsCCGGGCCTTCTGGGCGGGGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2841+27_2841+46delinsCCGGGCCTTCTGGGCGGGGA MANE Select	ENSP00000262407.5:n.2841+27_2841+46delins...
ENST00000648408.1:c.2272+27_2272+46delinsCCGGGCCTTCTGGGCGGGGA
ENST00000262407.5:c.2841+27_2841+46delinsCCGGGCCTTCTGGGCGGGGA	ENSP00000262407.5:n.2841+27_2841+46delins...
ENST00000587295.5:c.253+862_253+881delinsCCGGGCCTTCTGGGCGGGGA
ENST00000592462.5:n.2142_2161delinsCCGGGCCTTCTGGGCGGGGA
NM_000419.3:c.2841+27_2841+46delinsCCGGGCCTTCTGGGCGGGGA , LRG_479t1:c.2841+27_2841+46delinsCCGGGCCTTCTGGGCGGGGA	NP_000410.2:n.2841+27_2841+46delinsCCGGGC...
XM_011524749.1:c.2841+27_2841+46delinsCCGGGCCTTCTGGGCGGGGA	XP_011523051.1:n.2841+27_2841+46delinsCCG...
XM_011524750.1:c.2841+27_2841+46delinsCCGGGCCTTCTGGGCGGGGA	XP_011523052.1:n.2841+27_2841+46delinsCCG...
NM_000419.4:c.2841+27_2841+46delinsCCGGGCCTTCTGGGCGGGGA	NP_000410.2:n.2841+27_2841+46delinsCCGGGC...
NM_000419.5:c.2841+27_2841+46delinsCCGGGCCTTCTGGGCGGGGA MANE Select	NP_000410.2:n.2841+27_2841+46delinsCCGGGC...